Canonical Allele Identifier: CA383025915

Gene: SC5D

Linked Data

• MyVariant Identifiers: chr11:g.121174132C>A (hg19) ; chr11:g.121303423C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.121303423C>A , CM000673.2:g.121303423C>A	GRCh38
NC_000011.9:g.121174132C>A , CM000673.1:g.121174132C>A	GRCh37
NC_000011.8:g.120679342C>A	NCBI36
NG_009446.1:g.15745C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264027.9:c.48C>A MANE Select	ENSP00000264027.4:p.Tyr16Ter
ENST00000264027.8:c.48C>A	ENSP00000264027.4:p.Tyr16Ter
ENST00000392789.2:c.48C>A	ENSP00000376539.2:p.Tyr16Ter
ENST00000524683.5:n.104C>A
ENST00000527762.5:c.48C>A	ENSP00000436290.1:p.Tyr16Ter
ENST00000531140.1:n.116C>A
ENST00000534230.5:c.48C>A	ENSP00000432550.1:p.Tyr16Ter
ENST00000534455.5:n.194C>A
NM_001024956.2:c.48C>A	NP_001020127.1:p.Tyr16Ter
NM_006918.4:c.48C>A	NP_008849.2:p.Tyr16Ter
NM_006918.5:c.48C>A MANE Select	NP_008849.2:p.Tyr16Ter
NM_001024956.3:c.48C>A	NP_001020127.1:p.Tyr16Ter